Canonical Allele Identifier: CA1036731263

Gene: ACMSD

Linked Data

• dbSNP Id: rs1686841326
• gnomAD v3: 2-134842301-T-C
• gnomAD v4: 2-134842301-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.134842301T>C , CM000664.2:g.134842301T>C	GRCh38
NC_000002.11:g.135599871T>C , CM000664.1:g.135599871T>C	GRCh37
NC_000002.10:g.135316341T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356140.10:c.58-2932T>C MANE Select	ENSP00000348459.5:n.58-2932T>C
ENST00000356140.9:c.58-2932T>C	ENSP00000348459.5:n.58-2932T>C
ENST00000392928.5:c.-174-2064T>C	ENSP00000376659.1:n.-174-2064T>C
ENST00000485893.5:n.125-2932T>C
NM_001307983.1:c.-174-2064T>C	NP_001294912.1:n.-174-2064T>C
NM_138326.2:c.58-2932T>C	NP_612199.2:n.58-2932T>C
XM_005263586.3:c.58-2932T>C	XP_005263643.1:n.58-2932T>C
XM_005263588.3:c.-67-2932T>C	XP_005263645.1:n.-67-2932T>C
XM_005263589.3:c.-242-2058T>C	XP_005263646.1:n.-242-2058T>C
XM_011510592.1:c.-180-2058T>C	XP_011508894.1:n.-180-2058T>C
XM_005263586.4:c.58-2932T>C	XP_005263643.1:n.58-2932T>C
XM_005263588.4:c.-67-2932T>C	XP_005263645.1:n.-67-2932T>C
XM_005263589.4:c.-242-2058T>C	XP_005263646.1:n.-242-2058T>C
XM_011510592.2:c.-180-2058T>C	XP_011508894.1:n.-180-2058T>C
XM_017003325.1:c.-177-2061T>C	XP_016858814.1:n.-177-2061T>C
XM_017003326.1:c.-1233T>C	XP_016858815.1:n.-1233T>C
XM_024452690.1:c.-239-2061T>C	XP_024308458.1:n.-239-2061T>C
XM_024452691.1:c.-236-2064T>C	XP_024308459.1:n.-236-2064T>C
NM_138326.3:c.58-2932T>C MANE Select	NP_612199.2:n.58-2932T>C
NM_001307983.2:c.-174-2064T>C	NP_001294912.1:n.-174-2064T>C